potassium chloride

Generic: potassium chloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-218
Product ID 55289-218_4199ddf5-8d6b-0612-e063-6394a90a66f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077419
Listing Expiration 2026-12-31
Marketing Start 2008-08-25

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55289218
Hyphenated Format 55289-218

Supplemental Identifiers

RxCUI
312504
UPC
0355289218302
UNII
660YQ98I10

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA077419 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-218-30)
  • 270 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-218-94)
source: ndc

Packages (2)

55289-218-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-218-30) 55289-218-94 270 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-218-94)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4199ddf5-8d6b-0612-e063-6394a90a66f7", "openfda": {"upc": ["0355289218302"], "unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["35a1b03f-9716-4970-b9c2-998aa0923924"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-218-30)", "package_ndc": "55289-218-30", "marketing_start_date": "20110210"}, {"sample": false, "description": "270 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-218-94)", "package_ndc": "55289-218-94", "marketing_start_date": "20110210"}], "brand_name": "Potassium Chloride", "product_id": "55289-218_4199ddf5-8d6b-0612-e063-6394a90a66f7", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "55289-218", "generic_name": "Potassium Chloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA077419", "marketing_category": "ANDA", "marketing_start_date": "20080825", "listing_expiration_date": "20261231"}